Adipose Stromal Vascular Fraction Isolation: A Head-to-Head Comparison of Four Commercial Cell Separation Systems

被引:118
作者
Aronowitz, Joel A. [1 ]
Ellenhorn, Joshua D. I.
机构
[1] Univ So Calif, Keck Sch Med, Los Angeles, CA 90048 USA
关键词
STEM-CELLS; REGENERATIVE CELLS; ASSISTED LIPOTRANSFER; TISSUE;
D O I
10.1097/PRS.0b013e3182a80652
中图分类号
R61 [外科手术学];
学科分类号
100210 [外科学];
摘要
Background: Supplementation of fat grafts with stromal vascular fraction cells is an emerging technique used to improve graft reliability. A variety of systems for isolating stromal vascular fraction cells are commercially available. The lack of performance data obtained operating the systems in a standardized environment prevents objective assessment of performance. This prospective, blinded study compared performance of four commercially available stromal vascular fraction isolation systems when operated in a clinical outpatient surgery environment. Methods: Four different systems were compared: (1) PNC's Multi Station, (2) CHA Biotech Cha-Station, (3) Cytori Celution 800/CRS System, and (4) Medi-Khan's Lipokit with MaxStem. Identical lipoaspirate samples from five separate volunteer donors were used to evaluate system process time, viable cell yield, composition, residual enzyme, and operating costs. Results: The mean processing time ranged from 88 to 115 minutes. The highest mean number of viable nucleated cells was obtained using the Celution System (2.41 x 10(5) cells/g) followed by the Multi Station (1.07 x 10(5) cells/g). Lipokit and Cha-Station systems yielded nearly a log fewer nucleated cells (0.35 x 10(5) cells/g and 0.05 x 10(5) cells/g, respectively). The Celution System also yielded significantly more endothelial cells, CD34+/CD31-cells, and adipose-derived stem cells (colony-forming unit-fibroblast). Residual enzyme levels observed with the Multi Station, Cha-Station, and Lipokit, respectively, averaged 5.1-, 13.0-, and 57-fold higher than that observed with the Celution System. Conclusions: Although all systems generated measurable amounts of stromal vascular fraction, significant variability exists in the number, identity, and safety profiles of recovered viable cells. Side-by-side clinical trials will be required to establish the relevance of these differences.
引用
收藏
页码:932E / 939E
页数:8
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